KCF-S cluster No. 936 (10 metabolites)

Corresponding Phytochemical cluster No. 6



Metabolite list (10)

KNApSAcK ID name ChEMBL link CTD link # of proteins in
ChEMBL interaction
/ related OMIM
/ related KEGG DISEASE
# of genes in
CTD interaction
/ related diseases
figure
C00000621 External link 512 Chavicol
/ p-Hydroxyallylbenzene
CHEMBL108862
C00000776 External link 512 p-Hydroxybenzyl alcohol
C011276
C00001417 External link 512 Cactine
/ Anhalin
/ Anhaline
/ Hordenine
CHEMBL505789
C007964
1 / 0 / 0
C00001435 External link 512 Tyramine
CHEMBL11608
D014439
23 / 11 / 6 6 / 9
C00018213 External link 512 p-Hydroxyphenylacetaldoxime
C020363
C00027432 External link 512 N-Methyltyramine
C036244
C00029515 External link 512 p-Tyrosol
/ 4-(2-Hydroxyethyl)phenol
/ p-Hydroxyphenethyl alcohol
/ 2-(4-Hydroxyphenyl)ethanol
CHEMBL53566
C011867
6 / 3 / 5
C00029528 External link 512 4-Ethylphenol
CHEMBL108475
C042291
3 / 0 / 0 3 / 0
C00029532 External link 512 4-Hydroxybenzyl cyanide
/ p-Hydroxyphenylacetonitrile
/ 4-Hydroxy-benzeneacetonitrile
C026914
C00029533 External link 512 Gastrodigenin
/ 4-Methylolphenol
/ p-Hydroxybenzyl alcohol
/ 4-Hydroxybenzyl alcohol
CHEMBL202132
C018966
6 / 3 / 4 0 / 2

Human Protein / Gene in interactions

37 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
O94925 Glutaminase kidney isoform, mitochondrial Enzyme C00001417 C00001435 C00029515 0 / 0
P21917 D(4) dopamine receptor Dopamine receptor C00001435 0 / 0
P21728 D(1A) dopamine receptor Dopamine receptor C00001435 0 / 0
P27338 Amine oxidase [flavin-containing] B Oxidoreductase C00001435 0 / 0
Q9Y2D0 Carbonic anhydrase 5B, mitochondrial Lyase C00029515 0 / 0
P35218 Carbonic anhydrase 5A, mitochondrial Lyase C00029515 0 / 0
O15245 Solute carrier family 22 member 1 Drug uniporter C00001435 0 / 0
P00519 Tyrosine-protein kinase ABL1 Abl C00029533 1 / 2
P51649 Succinate-semialdehyde dehydrogenase, mitochondrial Oxidoreductase C00029533 1 / 1
P00918 Carbonic anhydrase 2 Lyase C00029515 1 / 2
P21397 Amine oxidase [flavin-containing] A Oxidoreductase C00001435 1 / 1
P06241 Tyrosine-protein kinase Fyn Src C00029533 0 / 0
P11712 Cytochrome P450 2C9 Cytochrome P450 2C9 C00001435 0 / 1
P14416 D(2) dopamine receptor Dopamine receptor C00001435 2 / 0
P00352 Retinal dehydrogenase 1 Enzyme C00001435 0 / 0
O75496 Geminin Unclassified protein C00001435 0 / 0
P50225 Sulfotransferase 1A1 Enzyme C00029528 0 / 0
O60656 UDP-glucuronosyltransferase 1-9 Enzyme C00029528 0 / 0
P49798 Regulator of G-protein signaling 4 Unclassified protein C00001435 2 / 0
P46098 5-hydroxytryptamine receptor 3A NS C00001435 0 / 0
P00915 Carbonic anhydrase 1 Lyase C00029515 0 / 0
P46108 Adapter molecule crk Unclassified protein C00029533 0 / 0
Q9Y468 Lethal(3)malignant brain tumor-like protein 1 Unclassified protein C00001435 0 / 0
P14679 Tyrosinase Oxidoreductase C00001435 4 / 2
P80404 4-aminobutyrate aminotransferase, mitochondrial Transferase C00029533 1 / 1
P08581 Hepatocyte growth factor receptor TK tyrosine-protein kinase MET subfamily C00029515 2 / 3
P62993 Growth factor receptor-bound protein 2 Other cytosolic protein C00029533 0 / 0
P56817 Beta-secretase 1 A1A C00001435 0 / 0
P05177 Cytochrome P450 1A2 Cytochrome P450 1A2 C00001435 0 / 0
P33261 Cytochrome P450 2C19 Cytochrome P450 2C19 C00001435 1 / 1
P08684 Cytochrome P450 3A4 Cytochrome P450 3A4 C00001435 0 / 1
Q96RJ0 Trace amine-associated receptor 1 Trace amine receptor C00001435 0 / 0
P19224 UDP-glucuronosyltransferase 1-6 Enzyme C00029528 0 / 0
B2RXH2 Lysine-specific demethylase 4E Enzyme C00001435 0 / 0
Q96KQ7 Histone-lysine N-methyltransferase EHMT2 Enzyme C00001435 0 / 0
O75751 Solute carrier family 22 member 3 Unclassified protein C00001435 0 / 0
P10635 Cytochrome P450 2D6 Cytochrome P450 2D6 C00001435 1 / 0

9 Gene in CTD interactions

gene gene name gene description KNApSAcK metabolite in interactions
2099 ESR1, ER, ESR, ESRA, ESTRR, Era, NR3A1 estrogen receptor 1 C00029528
2100 ESR2, ER-BETA, ESR-BETA, ESRB, ESTRB, Erb, NR3A2 estrogen receptor 2 (ER beta) C00029528
9970 NR1I3, CAR, CAR1, MB67 nuclear receptor subfamily 1, group I, member 3 C00029528
4128 MAOA, MAO-A monoamine oxidase A (EC:1.4.3.4) C00001435
6530 SLC6A2, NAT1, NET, NET1, SLC6A5 solute carrier family 6 (neurotransmitter transporter), member 2 C00001435
6531 SLC6A3, DAT, DAT1, PKDYS solute carrier family 6 (neurotransmitter transporter), member 3 C00001435
6532 SLC6A4, 5-HTT, 5-HTTLPR, 5HTT, HTT, OCD1, SERT, SERT1, hSERT solute carrier family 6 (neurotransmitter transporter), member 4 C00001435
6818 SULT1A3, HAST, HAST3, M-PST, ST1A3/ST1A4, ST1A5, STM, TL-PST sulfotransferase family, cytosolic, 1A, phenol-preferring, member 3 (EC:2.8.2.1) C00001435
134864 TAAR1, RP11-295F4.9, TA1, TAR1, TRAR1 trace amine associated receptor 1 C00001435

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (17)

OMIM preferred title UniProt
#103470 Albinism, ocular, with sensorineural deafness P14679
#203100 Albinism, oculocutaneous, type ia; oca1a P14679
#606952 Albinism, oculocutaneous, type ib; oca1b P14679
#103780 Alcohol dependence P14416
#300615 Brunner syndrome P21397
#609535 Drug metabolism, poor, cyp2c19-related P33261
#608902 Drug metabolism, poor, cyp2d6-related P10635
#613163 Gaba-transaminase deficiency P80404
#114550 Hepatocellular carcinoma P08581
#608232 Leukemia, chronic myeloid; cml P00519
#159900 Myoclonic dystonia P14416
#259730 Osteopetrosis, autosomal recessive 3; optb3 P00918
#605074 Renal cell carcinoma, papillary, 1; rccp1 P08581
#604906 Schizophrenia 9; sczd9 P49798
#181500 Schizophrenia; sczd P49798
#601800 Skin/hair/eye pigmentation, variation in, 3; shep3 P14679
#271980 Succinic semialdehyde dehydrogenase deficiency; ssadhd P51649

KEGG DISEASE (15)

KEGG name UniProt
H00001 Acute lymphoblastic leukemia (ALL) (precursor B lymphoblastic leukemia) P00519 (related)
P00519 (marker)
H00004 Chronic myeloid leukemia (CML) P00519 (related)
P00519 (marker)
H00241 Combined proximal and distal renal tubular acidosis (RTA type 3) P00918 (related)
H00436 Osteopetrosis P00918 (related)
H00018 Gastric cancer P08581 (related)
H00021 Renal cell carcinoma P08581 (related)
H00046 Cholangiocarcinoma P08581 (related)
H00036 Osteosarcoma P08684 (marker)
H01205 Coumarin resistance P11712 (related)
H00168 Oculocutaneous albinism (OCA) P14679 (related)
H00038 Malignant melanoma P14679 (marker)
H00548 Brunner syndrome P21397 (related)
H01171 Poor drug metabolism (PM) P33261 (related)
H00835 Succinic semialdehyde dehydrogenase (SSADH) deficiency P51649 (related)
H01257 GABA-transaminase deficiency P80404 (related)

Diseases related to CTD interactions

11 disease in interactions with metabolites

MESH or OMIM name KNApSAcK
metabolite
D000647 Amnesia C00029533
D007859 Learning Disorders C00029533
D009202 Cardiomyopathies C00001435
D002543 Cerebral Hemorrhage C00001435
D002637 Chest Pain C00001435
D006973 Hypertension C00001435
D007022 Hypotension C00001435
D008881 Migraine Disorders C00001435
D015878 Mydriasis C00001435
D011041 Poisoning C00001435
D013610 Tachycardia C00001435